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How to Conduct GCP Inspections / Audits at the Clinical Investigator Site

This course is intended to benefit regulatory good clinical practice (GCP) inspectors and sponsor auditors who audit clinical trials.
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Upon completion of this course, you will have an understanding of:

  1. The procedures involved in planning, conducting and reporting inspections/audits, specifically at clinical investigator sites.
  2. Some of the general principles described could also be used when conducting inspections at other sites e.g. those of the sponsors and contract research organisations (CRO).